Person who experienced the adverse event (patient)
| Event ID | CASE | I F COD | FOLL SEQ | IMAGE | EVENT DT | MFR DT | FDA DT | REPT COD | MFR NUM | MFR SNDR | AGE | AGE COD | GNDR COD | E SUB | WT | WT COD | REPT DT | OCCP COD | DEATH DT | TO MFR | CONFID | REPORTER COUNTRY |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 5689356 | 6335056 | F | 5689356-X | 20040520 | 20080321 | 20080331 | EXP | US-PFIZER INC-2007048046 | PFIZER INC | M | Y | 20080331 | LW | UNITED STATES |
Drug(s) used by person
| Event ID | DRUG SEQ | ROLE COD | DRUGNAME | VAL VBM | ROUTE | DOSE VBM | DECHAL | RECHAL | LOT NUM | EXP DT | NDA NUM |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 5689356 | 1009729008 | PS | BEXTRA | 1 | ORAL | 021341 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 5689356 | 1009729008 | BACK PAIN |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 5689356 | HO |
| 5689356 | OT |
Reactions reported
| Event ID | PT |
|---|---|
| 5689356 | MYOCARDIAL INFARCTION |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |